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Studies on antiulcer drugs. V. Synthesis and antiulcer activity of aralkylbenzazoles.

作者信息

Katsura Y, Inoue Y, Tomoi M, Takasugi H

机构信息

New Drug Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1992 Aug;40(8):2062-74. doi: 10.1248/cpb.40.2062.

Abstract

A series of 2-alkylamino-5- or 6-aralkyl-substituted benzazoles were synthesized and tested for histamine H2-receptor antagonist and anti-stress ulcer activities. These new compounds showed little or no histamine H2-receptor antagonist activity in contrast to imidazo[1,2-a]pyridine analogues (I). On antiulcer assay, however, some pyridine derivatives (II) exerted higher activity than the reference compounds, sofalcone, sucralfate and cimetidine. The structure-activity relationships of these compounds are discussed.

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